Genome-wide association study of shared components of reading disability and language impairment

Alleles of a Polymorphic ETV6 Binding Site in DCDC2 Confer Risk of Reading and Language Impairment

(2013) Natalie R. Powers et al.   AMERICAN JOURNAL OF HUMAN GENETICS

DNA Evidence for Strong Genome-Wide Pleiotropy of Cognitive and Learning Abilities

(2013) Maciej Trzaskowski et al.   BEHAVIOR GENETICS

A genome-wide association study for reading and language abilities in two population cohorts

(2013) M. Luciano et al.   GENES BRAIN AND BEHAVIOR

Imaging-genetics in dyslexia: Connecting risk genetic variants to brain neuroimaging and ultimately to reading impairments

(2013) John D. Eicher et al.   MOLECULAR GENETICS AND METABOLISM

Cognition assessment using the NIH Toolbox

(2013) S. Weintraub et al.   NEUROLOGY

BCL9 and C9orf5 Are Associated with Negative Symptoms in Schizophrenia: Meta-Analysis of Two Genome-Wide Association Studies

(2013) Chun Xu et al.   PLoS One

Three Dyslexia Susceptibility Genes, DYX1C1, DCDC2, and KIAA0319, Affect Temporo-Parietal White Matter Structure

(2012) Fahimeh Darki et al.   BIOLOGICAL PSYCHIATRY

A tractography study in dyslexia: neuroanatomic correlates of orthographic, phonological and speech processing

(2012) M. Vandermosten et al.   BRAIN

Neuroanatomical Assessment of Biological Maturity

(2012) Timothy T. Brown et al.   CURRENT BIOLOGY

Decoding the genetics of speech and language

(2012) Sarah A Graham et al.   CURRENT OPINION IN NEUROBIOLOGY

COL4A2 mutation associated with familial porencephaly and small-vessel disease

(2012) Elly Verbeek et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Cohort Profile: The ‘Children of the 90s’—the index offspring of the Avon Longitudinal Study of Parents and Children

(2012) Andy Boyd et al.   INTERNATIONAL JOURNAL OF EPIDEMIOLOGY

Genetic Variants of FOXP2 and KIAA0319/TTRAP/THEM2 Locus Are Associated with Altered Brain Activation in Distinct Language-Related Regions

(2012) P. Pinel et al.   JOURNAL OF NEUROSCIENCE

Developmental dyslexia

(2012) Robin L Peterson et al.   LANCET

Variants in the DYX2 locus are associated with altered brain activation in reading-related brain regions in subjects with reading disability

(2012) Natalie Cope et al.   NEUROIMAGE

FreeSurfer

(2012) Bruce Fischl   NEUROIMAGE

The Dyslexia Candidate Locus on 2p12 Is Associated with General Cognitive Ability and White Matter Structure

(2012) Thomas S. Scerri et al.   PLoS One

Multimodal imaging of the self-regulating developing brain

(2012) A. M. Fjell et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

Long-term influence of normal variation in neonatal characteristics on human brain development

(2012) K. B. Walhovd et al.   PROCEEDINGS OF THE NATIONAL ACADEMY OF SCIENCES OF THE UNITED STATES OF AMERICA

De Novo and Inherited Mutations in COL4A2, Encoding the Type IV Collagen α2 Chain Cause Porencephaly

(2011) Yuriko Yoneda et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Integrated Genome-Wide Association Study Findings: Identification of a Neurodevelopmental Network for Attention Deficit Hyperactivity Disorder

(2011) Geert Poelmans et al.   AMERICAN JOURNAL OF PSYCHIATRY

DCDC2, KIAA0319 and CMIP Are Associated with Reading-Related Traits

(2011) Tom S. Scerri et al.   BIOLOGICAL PSYCHIATRY

Imaging genetics of FOXP2 in dyslexia

(2011) Arndt Wilcke et al.   EUROPEAN JOURNAL OF HUMAN GENETICS

Foxp2 Regulates Gene Networks Implicated in Neurite Outgrowth in the Developing Brain

(2011) Sonja C. Vernes et al.   PLoS Genetics

A Versatile Gene-Based Test for Genome-wide Association Studies

(2010) Jimmy Z. Liu et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Investigation of Dyslexia and SLI Risk Variants in Reading- and Language-Impaired Subjects

(2010) D. F. Newbury et al.   BEHAVIOR GENETICS

A Dyslexia-Associated Variant in DCDC2 Changes Gene Expression

(2010) Haiying Meng et al.   BEHAVIOR GENETICS

Replication of CNTNAP2 association with nonword repetition and support for FOXP2 association with timed reading and motor activities in a dyslexia family sample

(2010) Beate Peter et al.   Journal of Neurodevelopmental Disorders

Normal variation in fronto-occipital circuitry and cerebellar structure with an autism-associated polymorphism of CNTNAP2

(2010) Geoffrey C.Y. Tan et al.   NEUROIMAGE

Altered Functional Connectivity in Frontal Lobe Circuits Is Associated with Variation in the Autism Risk Gene CNTNAP2

(2010) A. A. Scott-Van Zeeland et al.   Science Translational Medicine

CMIP and ATP2C2 Modulate Phonological Short-Term Memory in Language Impairment

(2009) Dianne F. Newbury et al.   AMERICAN JOURNAL OF HUMAN GENETICS

Language pathway abnormalities in schizophrenia: a review of fMRI and other imaging studies

(2009) Xiaobo Li et al.   CURRENT OPINION IN PSYCHIATRY

Genetics of developmental dyslexia

(2009) Thomas S. Scerri et al.   EUROPEAN CHILD & ADOLESCENT PSYCHIATRY

Fast model-based estimation of ancestry in unrelated individuals

(2009) D. H. Alexander et al.   GENOME RESEARCH

Convergent genetic linkage and associations to language, speech and reading measures in families of probands with Specific Language Impairment

(2009) Mabel L. Rice et al.   Journal of Neurodevelopmental Disorders

Efficient correction of inhomogeneous static magnetic field-induced distortion in Echo Planar Imaging

(2009) Dominic Holland et al.   NEUROIMAGE

A Common Variant Associated with Dyslexia Reduces Expression of the KIAA0319 Gene

(2009) Megan Y. Dennis et al.   PLoS Genetics

Association of theKIAA0319Dyslexia Susceptibility Gene With Reading Skills in the General Population

(2008) Silvia Paracchini et al.   AMERICAN JOURNAL OF PSYCHIATRY

Relations Among Speech, Language, and Reading Disorders

(2008) Bruce F. Pennington et al.   Annual Review of Psychology

Automated white-matter tractography using a probabilistic diffusion tensor atlas: Application to temporal lobe epilepsy

(2008) Donald J. Hagler et al.   HUMAN BRAIN MAPPING

Investigation of interaction between DCDC2 and KIAA0319 in a large German dyslexia sample

(2008) Kerstin U. Ludwig et al.   JOURNAL OF NEURAL TRANSMISSION